EP3180290B1 - Verfahren zur extraktion und trennung von seltenerdelementen - Google Patents

Verfahren zur extraktion und trennung von seltenerdelementen Download PDF

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EP3180290B1
EP3180290B1 EP15832278.4A EP15832278A EP3180290B1 EP 3180290 B1 EP3180290 B1 EP 3180290B1 EP 15832278 A EP15832278 A EP 15832278A EP 3180290 B1 EP3180290 B1 EP 3180290B1
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Prior art keywords
rare earth
concentrate
solution
ore
oxide
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French (fr)
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EP3180290A4 (de
EP3180290A1 (de
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Joseph Brewer
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Rare Earth Salts Separation And Refining LLC
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Rare Earth Salts Separation And Refining LLC
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Priority to SI201531289T priority Critical patent/SI3180290T1/sl
Priority to PL15832278T priority patent/PL3180290T3/pl
Priority to RS20200850A priority patent/RS60628B1/sr
Publication of EP3180290A1 publication Critical patent/EP3180290A1/de
Publication of EP3180290A4 publication Critical patent/EP3180290A4/de
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Priority to HRP20201123TT priority patent/HRP20201123T1/hr
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    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
    • C01F17/00—Compounds of rare earth metals
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B3/00—Extraction of metal compounds from ores or concentrates by wet processes
    • C22B3/04—Extraction of metal compounds from ores or concentrates by wet processes by leaching
    • C22B3/06—Extraction of metal compounds from ores or concentrates by wet processes by leaching in inorganic acid solutions, e.g. with acids generated in situ; in inorganic salt solutions other than ammonium salt solutions
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
    • C01F17/00—Compounds of rare earth metals
    • C01F17/20—Compounds containing only rare earth metals as the metal element
    • C01F17/206—Compounds containing only rare earth metals as the metal element oxide or hydroxide being the only anion
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
    • C01F17/00—Compounds of rare earth metals
    • C01F17/20—Compounds containing only rare earth metals as the metal element
    • C01F17/253—Halides
    • C01F17/259—Oxyhalides
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B3/00—Extraction of metal compounds from ores or concentrates by wet processes
    • C22B3/20—Treatment or purification of solutions, e.g. obtained by leaching
    • C22B3/44—Treatment or purification of solutions, e.g. obtained by leaching by chemical processes
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B59/00—Obtaining rare earth metals
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25C—PROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
    • C25C1/00—Electrolytic production, recovery or refining of metals by electrolysis of solutions
    • C25C1/22—Electrolytic production, recovery or refining of metals by electrolysis of solutions of metals not provided for in groups C25C1/02 - C25C1/20
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25C—PROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
    • C25C7/00—Constructional parts, or assemblies thereof, of cells; Servicing or operating of cells
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00—Technologies related to metal processing
    • Y02P10/20—Recycling

Definitions

  • the present invention is related in general to recovery, extraction and/or separation of rare earth elements (REE), and in particular to a method and apparatus for extracting and separating rare earth elements from rare earth containing materials (e.g., ore, tailings or product of recycling).
  • REE rare earth elements
  • Rare earth elements principally include the lanthanide series of the periodic table, but the term can also incorporate scandium and yttrium.
  • Exemplary rare earth elements include: lanthanum (La), cerium (Ce), praseodymium (Pr), neodymium (Nd), samarium (Sm), europium (Eu), gadolinium (Gd), terbium (Tb), dysprosium (Dy), holmium (Ho), erbium (Er), thulium (Tm), ytterbium (Yb), lutetium (Lu), scandium (Sc) and yttrium (Y).
  • La lanthanum
  • Ce cerium
  • Pr praseodymium
  • Nd neodymium
  • Sm samarium
  • Eu europium
  • Gd gadolinium
  • Tb terbium
  • Dy dysprosium
  • Ho holmium
  • Er erbium
  • Rare earth elements can include light rare earth elements, medium rare earth elements, and/or heavy rare earth elements.
  • Exemplary light rare earth elements include La, Ce, Pr, Nd, and Pm.
  • Exemplary medium rare earth elements include Sm, Eu, and Gd.
  • Exemplary heavy rare earth elements include Sc, Tb, Dy, Ho, Er, Tm, Yb, Lu, and Y.
  • Rare earth elements that are recovered from ore/tailings can have a number of applications.
  • some of these ores/tailings contain Y, a heavy rare earth element that can be used in compact fluorescent light bulbs.
  • the ores/tailings can also contain Nd, a light rare earth element that can be used in permanent magnet motors in hybrid vehicles, wind turbines, and computer disk drives.
  • Other applications for rare earth elements can include, for example, use in aerospace components, high refractive index glass, flint, batteries, catalysts, polishes, lasers, x-ray machines and capacitors.
  • the components containing rare earths utilized in these previously mentioned applications can also be recycled and the rare earths recovered from them.
  • the preferred embodiment of the present invention provides a method for extracting and separating rare earth elements.
  • the present embodiment discloses a method for extracting and separating rare earth elements.
  • the process starts with providing a rare earth bearing material (e.g., ore, tailing or product of recycling).
  • the rare earth ore is leached with at least one mineral acid such as, nitric acid (HNO 3 ) or hydrochloric acid (HCl) to form a leach solution.
  • the at least one mineral acid can be of any concentration with a pH of less than 1.
  • the leach mixture contains the leach solution which includes at least rare earth ions and a solid material.
  • the leach solution may also include at least one metal ion.
  • the at least one metal ion can include at least one aluminum ion, at least one zinc ion, at least one copper ion, at least one nickel ion, at least one titanium ion and/or at least one iron ion.
  • the leach solution may be heated to improve the extraction of the rare earths from the rare earth bearing material.
  • the solid material is separated from the liquid/solid residue and a liquid-rare earth ion leachate solution is obtained.
  • the solid material is removed as waste or for the recovery of the iron (Fe) or other materials by any desired process.
  • the liquid-rare earth ion leachate solution is treated to recover the rare earth elements.
  • the at least one metal ion e.g. iron
  • the at least one metal ion is precipitated from the leach solution by titrating leach solution with magnesium oxide (MgO) by adjusting the leach solution to a pH of about 1 to a pH of about 4.
  • MgO magnesium oxide
  • the liquid-rare earth concentrate is then treated by either oxalic acid addition to precipitate a rare earth oxalate concentrate or by titration to a pH of 7 by magnesium oxide or carbonate to generate a rare earth hydroxide or carbonate concentrate.
  • the rare earth concentrate is precipitated from the rare earth leach solution as one or more insoluble rare earth compounds.
  • a rare earth bearing ore or tailings such as monazite, is added to the at least one mineral acid, such as nitric acid.
  • the ore or tailings and acid are mixed and heated to dissolve the rare earth bearing materials from the ore or tailings.
  • the leachant solution impregnated with rare earths is separated from the solid rare earth depleted tailings or ore.
  • the leachant solution is then titrated with MgO to precipitate out an insoluble transition metal compound such as iron phosphate or iron hydroxide.
  • the appropriate amount of oxalate compound, such as oxalic acid or ammonium oxalate can be added to precipitate a rare earth oxalate concentrate or the solution can be titrated to pH 7 by magnesium oxide or magnesium carbonate to precipitate out a rare earth hydroxide or carbonate concentrate.
  • the rare earth ore such as ionic clay
  • an at least one mineral acid solution containing an oxalate compound such as ammonium oxalate is stirred and the rare earth depleted ionic clay is separated from the rare earth impregnated solution.
  • the rare earth impregnated solution is then titrated with magnesium oxide or other base to produce a rare earth oxalate concentrate which may contain other metal other than rare earths in high concentration.
  • the precipitated rare earth concentrate produces rare earth oxalates and is then heated in air (calcined) to at least 350°C to produce oxide of rare earth concentrate.
  • the rare earth elements can be insolubilized out of the solution and can be found as an ion associated to an hydroxide or a salt or hydrates thereof.
  • magnesium nitrate (Mg(NO 3 ) 2 ) is removed from solution by evaporation of the water component.
  • the magnesium nitrate (MgNO 3 ) is then thermally decomposed by raising the temperature of the salt to form magnesium oxide (MgO) and gaseous nitric oxides (NO X ).
  • the nitricoxides (NO X ) are then bubbled through water to regenerate the nitric acid (HNO 3 ).
  • the nitric values are removed, leaving the magnesium oxide (MgO).
  • the regenerated nitric acid is recycled to the leaching step for further use.
  • the rare earth oxide concentrate is mixed with an ammonium salt, for example ammonium chloride, ammonium bromide or ammonium iodide at a ratio ranging from 1:0.5 (oxide:ammonium salt) to 1:10 with the optimal conditions being between 1:2 and 1:4.
  • the mixture is heated at a temperature between 200°C and 250°C in dry air or nitrogen flow until there is no more apparent color change in the material. Preferably, the temperature is approximately 200°C.
  • the temperature is then increased to 250°C to 350 °C under dry air or nitrogen with mixing until the sublimation of the excess ammonium salt is complete.
  • the resulting material is a mixture of anhydrous rare earth salts.
  • the anhydrous rare earth salts are utilized as provided in an aqueous solution for the separations process. Non-soluble materials from the conversion are typically transition metal impurities in the rare earth concentrate.
  • the rare earth elements are separated from the aqueous solution by means of an electrowinning process using a sacrificial anode.
  • electrowinning process refers to an electrodeposition of metals from solutions containing the metals onto a plate or wire mesh thereby allowing purification of a metal.
  • a potential is applied between a cathode and the sacrificial anode.
  • the cathode is a relatively inert metal, such as steel or molybdenum.
  • the sacrificial anode is aluminum. The potential is then varied to increasing potentials to allow the sequential deposition of the rare earth elements.
  • the potential used can vary from an electrolytic cell to over 1.0V, for example, with a typical range between 0.1V and 0.7V.
  • the initial electrode position occurs at approximately 0.2V and yields a material that is dominated by scandium and heavy rare earth elements. Temperature may also be adjusted from 1° C to 35° C to facilitate the separations process.
  • the electrowinning process may be accomplished in any number of cell configurations, including a single cell with no junctions or a cell with one or more liquid junctions such as, salt bridges or membrane.
  • a cell with multiple junctions would be a cell in which the anode and cathodes are alternated and separated by an anion membrane.
  • the anodic half cells with the aluminum plates are defined as aluminum cells and contain a sodium chloride aqueous solution ranging from 0M to saturated or the same sodium chloride solution with aluminum chloride ranging from 0.001 to 1M.
  • the cathodic half cells with the inert metal plates contain the rare earth salt aqueous solution.
  • the inert metal plates are steel or molybdenum.
  • the membranes prevent migration of cations and water between the rare earth elements and aluminum cells. However, the membrane allows movement of anions, such as chloride, bromide, iodide or nitrate, and hydrogen ions.
  • a rare earth plating process is facilitated by the oxidation of the aluminum plates into the aqueous sodium chloride solution.
  • a rare earth element is reduced and deposited in the corresponding rare earth cell.
  • the anions diffuse through the membrane and complex with the aluminum ions in the aluminum cell to maintain the appropriate charge balance.
  • the plated material spontaneously oxidizes and is then removed from the electrode and processed through the rare earth oxide concentrate to salt conversion process.
  • the plated material is thermally treated with an ammonium salt in between iterations.
  • the solution containing the remaining rare earth ions from the iterations is added back into either a main heavy rare earth ion depleted feed stream or a purification stream for a second rare earth element to be separated, depending on the composition on the solution.
  • the heavy rare earth depleted solution from the original electrodeposition is then passed into a second cell for the separation of the next rare earth element in the sequence.
  • the process of separation and purification is continued for each of sixteen rare earth elements of interest, for example, lanthanum (La), cerium (Ce), praseodymium (Pr), neodymium (Nd), samarium (Sm), europium (Eu), gadolinium (Gd), terbium (Tb), dysprosium (Dy), holmium (Ho), erbium (Er), thulium (Tm), ytterbium (Yb), lutetium (Lu), scandium (Sc) and yttrium (Y).
  • the potential of each separation cell is optimized to yield the rare earth element of interest plus one to two major impurity elements.
  • the purifying cells are then used to concentrate the rare earth element of interest while minimizing the amount of the impurity elements.
  • a method for extracting and separating rare earth elements is disclosed. Initially, a rare earth -containing ore or tailings is provided and the rare earth-containing ore or tailings is processed to sub-60 mesh utilizing mechanical grinding to form powdered ore. The powdered ore is leached using a mineral acid, for example, nitric acid (HNO 3 ) to form a leach solution having at least one metal ion, rare earth elements and a solid material. The leaching process is followed by a liquid-solid separation step in which the solid material is separated from the leach solution to form aqueous rare earth concentrate.
  • a mineral acid for example, nitric acid (HNO 3 )
  • the aqueous rare earth concentrate is precipitated to selectively remove the at least one metal ion from the leach solution and obtain a precipitate of the rare earth elements in the form of rare earth oxalates.
  • the precipitate of the rare earth elements or rare earth oxalates is heated in air to form an oxide of the rare earth elements.
  • the rare earth oxide is mixed with an ammonium salt and heated in a dry air/nitrogen at a rare earth conversion step.
  • a mixture of anhydrous rare earth salts is formed and is provided in an aqueous solution.
  • the rare earth elements are separated from the aqueous solution by means of an electrowinning process. During the electrowinning process the rare earth elements are plated from the aqueous solution using a sacrificial anode and are removed as oxidized rare earth compounds.
  • FIG. 1 is a basic schematic flow diagram of a method for extracting and separating rare earth elements.
  • the process starts with providing a rare earth bearing material (e.g., ore, tailings or product of recycling).
  • the rare earth ore or tailings 100 is leached 102 with at least one mineral acid such as, nitric acid (HNO 3 ) or hydrochloric acid (HCl) 104 to form a leach solution.
  • the at least one mineral acid can be any concentration with a pH less than 1.
  • the at least one mineral acid used for leaching the rare earth ore can be HCl, H 2 SO 4 , HNO 3 or mixtures thereof. More than one acid can be used as a mixture or separately. Solutions made with these acids can be used at various concentrations.
  • a rare earth chelating agent such as an oxalate compound may also be added to the leaching acid prior to the addition of the rare earth bearing ore/tailings.
  • the rare earth ore 100 may be stockpiled for processing, or they may be blended with other ores, metallurgical wastes, or other rare earth-bearing materials. When required, the ores are ground or powdered or reduced in size to effectively dissolve the ore in the at least one mineral acid during the leaching step 102.
  • the leach solution includes at least one rare earth 118 and a solid material 110.
  • the leach solution may also contain at least one metal ion.
  • the at least one metal ion can include at least one aluminum ion, at least one zinc ion, at least one copper ion, at least one nickel ion, at least one titanium ion and/or at least one iron ion.
  • the leach solution is optionally heated 106 to form a liquid/solid residue 108.
  • the leaching step 102 and heating step 106 can be carried out in the same vessel, or in separate vessels.
  • the solid material 110 is separated from the liquid/solid residue 108 and an aqueous-rare earth concentrate 112 is formed.
  • the solid material 110 is removed for the recovery of the iron (Fe) or other materials by any desired process.
  • the aqueous-rare earth concentrate 112 is treated to recover the rare earths 118.
  • the at least one metal ion is optionally precipitated 122 from the leach solution by titrating leach solution with magnesium oxide (MgO) 120 by adjusting the leach solution to a pH of about 1 to a pH of about 4.
  • MgO magnesium oxide
  • the precipitate is separated via filtration, centrifuge or decanting centrifuge.
  • the aqueous-rare earth concentrate 112 is then treated with either the appropriate oxalate bearing compound to precipitate out a rare earth oxalate concentrate or basic magnesium compound to pH 7 to precipitate out a rare earth hydroxide or carbonate concentrate.
  • the precipitated rare earth concentrate 122 produces rare earth oxalates, hydroxides or carbonates and is then heated at 130 in air (calcined) to at least 350°C or hotter to produce oxide of rare earth concentrate at 114.
  • the rare earths 118 can be insolubilized from the solution and can be found as an ion associated to an hydroxide or a salt or hydrates thereof.
  • magnesium nitrate (Mg(NO 3 ) 2 ) solution is heated at 124 to remove the water.
  • the magnesium nitrate (Mg(NO 3 ) 2 ) 124 is then thermally decomposed by raising the temperature of the salt to form magnesium oxide (MgO) and gaseous nitric oxides (NO X ) at 120 and 128 respectively as shown in FIG. 2 .
  • the nitric oxides (NO X ) 128 are then bubbled through water to regenerate the nitric acid (HNO 3 ) at 104.
  • the nitric values 126 are removed, leaving the magnesium oxide (MgO) 120.
  • the removed nitric acid 126, with nitric oxides (NO X ) 128 added, as necessary, is recycled to the leaching step 102 or to the nitric acid 104 recycle process for further use.
  • the rare earth oxide concentrate 114 is mixed with an ammonium salt 134 such as for example ammonium chloride, ammonium bromide or ammonium iodide at a ratio ranging from 1:0.5 (oxide: ammonium salt) to 1:10 with the optimal conditions being between 1:1 and 1:2.
  • the mixture is heated at a temperature between 200°C and 250°C in dry air or nitrogen flow until there is no more apparent color change in the material. Preferably, the temperature is approximately 200°C.
  • the temperature is then increased to 250°C to 350°C under dry air or nitrogen 132 with mixing until the sublimation of the excess ammonium salt 134 is complete.
  • the resulting material is a mixture of anhydrous rare earth salts 116.
  • the anhydrous rare earth salts 116 are utilized as provided in an aqueous solution.
  • the ammonium from the conversion process is bubbled through hydrochloric acid (HCl) to regenerate ammonium chloride.
  • HCl hydrochloric acid
  • the excess ammonium chloride is condensed out of the gas phase for recovery and is reused in the rare earth conversion process.
  • the rare earths 118 are separated from the aqueous solution by means of an electrowinning process 136 using a sacrificial anode.
  • electrowinning refers to an electrodeposition of metals from their ores onto a plate or wire mesh thereby allows purification of a non-ferrous metal.
  • a potential is applied between a cathode and the sacrificial anode.
  • the cathode is a relatively inert metal, such as steel or molybdenum.
  • the sacrificial anode is aluminum. The potential is then varied to increasing potentials to allow the sequential deposition of the rare earth elements 118.
  • the potential used can vary from an electrolytic cell to over 1.0V, for example, with a typical range between 0.2V and 0.7V.
  • the initial electrode position occurs at approximately 0.2V and yields a material that is dominated by scandium and heavy rare earth elements. Temperature may also be adjusted from 1° C to 35° C to facilitate the separations process.
  • the electrowinning process 136 may be accomplished in any number of cell configurations, including a single cell with no junctions or a cell with one or core liquid junctions (salt bridges or membrane).
  • a cell with multiple junctions would be a cell in which the anode and cathodes are alternated and separated by an anion membrane.
  • the anodic half cells with the aluminum plates is defined as aluminum cells and contains a sodium chloride aqueous solution ranging from 0-M to saturated or the same sodium chloride solution with aluminum chloride ranging from 0.001 to 1M.
  • the cathodic half cells with the inert metal plates contain the rare earth salt aqueous solution.
  • the inert metal plates are steel or molybdenum.
  • the membranes prevent migration of cations and water between the rare earth 118 and aluminum cells. However, the membrane allows movement of anions, such as chloride, bromide, iodide or nitrate, and hydrogen ions.
  • a rare earth plating process is facilitated by the oxidation of the aluminum plates into the aqueous sodium chloride solution.
  • a rare earth element 118 is reduced and deposited in the corresponding rare earth cell.
  • the anions diffuse through the membrane and complex with the aluminum ions in the aluminum cell to maintain the appropriate charge balance.
  • the plated material spontaneously oxidizes and is then processed through the rare earth oxide concentrate to salt conversion process as illustrated in FIG. 2 . This process is repeated for a total of 10-30 iterations to produce a 99.9% pure rare earth element 118, mostly an oxide of the rare earth element 118.
  • the plated material is thermally treated with ammonium salt in between the iterations.
  • the solution containing the impurity elements formed from the iterations is added back into either a main heavy rare earth depleted feed stream or a purification stream for a second rare earth element to be separated, depending on the composition on the solution.
  • the heavy rare earth depleted solution from the original electrodeposition is then passed into a second cell for the separation of the second rare earth element in the sequence.
  • each of the sixteen rare earth elements 118 of interest for example, lanthanum (La), cerium (Ce), praseodymium (Pr), neodymium (Nd), samarium (Sm), europium (Eu), gadolinium (Gd), terbium (Tb), dysprosium (Dy), holmium (Ho), erbium (Er), thulium (Tm), ytterbium (Yb), lutetium (Lu), scandium (Sc) and yttrium (Y).
  • the potential of each separation cell is optimized to yield the rare earth element(s) 118 of interest plus several other major impurity elements depending on the iteration.
  • the purifying cells are then used to concentrate the rare earth element 118 of interest while minimizing the amount of the impurity elements.
  • FIG. 3 is a flowchart illustrating a method 140 for extracting and separating rare earth elements in accordance with the preferred embodiment of the present invention.
  • a rare earth-containing (RE-containing) ore/tailings is provided as indicated at block 142.
  • the rare earth-containing ore/tailings is processed to sub 60 mesh utilizing mechanical grinding to form powdered ore as indicated at block 144.
  • the grinding step 144 is followed with a leaching step as indicated at block 146.
  • Leaching step 146 can be any method, process, or system that enables a rare earth element to be leached from a rare earth containing material. Typically, the leaching step 146 utilizes an acid to leach a rare earth element from a rare earth containing material.
  • leaching step 146 can employ a leaching apparatus such as for example, a heap leach, a vat leach, a tank leach, a pad leach, a leach vessel or any other leaching technology useful for leaching a rare earth element from a rare earth containing material.
  • leaching step 146 may be conducted at any suitable pressure, temperature, and/or oxygen content.
  • Leaching step 146 can employ one of a high temperature, a medium temperature, or a low temperature, combined with one of high pressure, or atmospheric pressure. Leaching step 146 may utilize conventional atmospheric or pressure leaching, for example but not limited to, low, medium or high temperature pressure leaching.
  • pressure leaching refers to a rare earth element recovery process in which the rare earth containing material is contacted with an acidic solution and oxygen under conditions of elevated temperature and pressure.
  • the leaching step 146 preferably includes a mineral acid, for example, nitric acid (HNO 3 ).
  • the mineral acid is hydrochloric acid (HCl).
  • the mineral acid is selected based on a specific application for the rare earth elements.
  • the concentration and quantity of the nitric acid or hydrochloric acid depend on the metal-containing ore. In these embodiments, the concentration of mineral acid is such that the pH is less than 1. In steps 144 and 146, there is no crushing and separating of the metal-containing ore into valuable substances or waste.
  • the leaching step 146 provides a leach solution comprising at least one metal ion, rare earths and a solid material as indicated at block 148.
  • the leaching step 146 is followed by a liquid-solid separation step in which the solid material is separated from the leach solution to form aqueous-metal concentrate as indicated at block 150.
  • the aqueous-metal concentrate can be precipitated to selectively remove the at least one metal ion from the leach solution and obtain a precipitate of the rare earth elements in the form of rare earth oxalates or hydroxides as indicated at block 152.
  • the precipitate of the rare earth hydroxides or rare earth oxalates is heated in air to form an oxide of the rare earth elements as indicated at block 154.
  • the rare earth oxide is mixed with an ammonium salt and heated in a dry air/nitrogen at a rare earth conversion step as indicated at block 156.
  • a mixture of anhydrous rare earth salts is formed and is provided in an aqueous solution as indicated at block 158.
  • the rare earth elements are separated from the aqueous solution by means of an electrowinning process as indicated at block 160.
  • the electrowinning process 160 the rare earth elements are plated from the aqueous solution using a sacrificial anode.
  • the rare earths 118 are extracted from rare earth bearing ores 100 and tailings.
  • the extraction process can be used for the recovery of rare earth elements 118 from industrial products such as magnets or phosphors.
  • the leaching step 102 includes any concentration of acid.
  • the rare earth elements 118 are removed from the nitric acid 104 leach solution by titration with magnesium oxide (MgO) 120 and the pH adjusted solution is then spray dried to recover the magnesium nitrate (Mg(NO 3 ) 2 ) 124 to MgO 120 and nitric oxide (NO X ) 128.
  • the nitric oxide (NO X ) 128 is then bubbled through water to recover the acid.
  • the rare earth elements 118 are in a solid solution or concentrate instead of individual rare earth elements.
  • the time is decreased from 10 hours per Gerd Meyer process to 6 hours and temperature is decreased from 230°C to 200°C.
  • the rare earth conversion step is run under dry air/nitrogen 132 instead of dynamic vacuum as water causes the oxidation of the rare earth chloride to an oxychloride.
  • the method is used to remove impurity fractions from the liquid-rare earth concentrate 112 generated from the extraction and the plating process.
  • the excess ammonium chloride is condensed out of the gas phase for recovery and reuse.
  • the ammonia gas is bubbled through water to recover and is reacted with HCl to regenerate ammonium chloride and is reused in the rare earth conversion process.

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Claims (12)

  1. Verfahren zum Extrahieren und Trennen von Seltene-Erdenelementen, wobei das Verfahren die folgenden Schritte aufweist:
    Vorsehen eines Erzes, welches ein Seltene-Erdenelement enthält;
    Mahlen des Erzes, welches ein Seltene-Erdenelement enthält, um pulverförmiges Erz zu bilden;
    Auswaschen bzw. Laugen des pulverförmigen Erzes mit mindestens einer Mineralsäure, um eine Waschlösung zu bilden, welche eine Seltene-Erdenelement und ein festes Material aufweist;
    Trennen des festen Materials von der Waschlösung, um ein wässriges Seltene-Erdenkonzentrat zu bilden;
    Ausscheiden bzw. Fällen des wässrigen Seltene-Erdenkonzentrates, um selektiv das seltene-Erdenelement aus der Waschlösung zu entfernen und um eine Ausscheidung bzw. Ausfällung des Seltene-Erdenelementes zu erhalten;
    Aufheizen der Ausscheidung des Seltene-Erdenelementes in Luft, um ein Oxyd des Seltene-Erdenelementes zu bilden;
    Mischen und Aufheizen des Oxydes des Seltene-Erdenelementes mit einem Ammoniumsalz, um anhydrische bzw. wasserfreie Seltene-Erdensalze zu bilden;
    Formen einer Mischung der anhydrischen Seltene-Erdensalze in einer wässrigen Lösung; und
    Trennen des Seltene-Erdenelementes von der wässrigen Lösung durch ein Stromgewinnungsverfahren unter Verwendung einer Opferanode.
  2. Verfahren zum Extrahieren von Seltene-Erdenelementen aus einem Erz, welches Seltene Erden enthält, wobei das Verfahren die folgenden Schritte aufweist:
    Mahlen des Erzes, welches Seltene Erden enthält, um pulverförmiges Erz zu bilden;
    Auswaschen bzw. Laugen des pulverförmigen Erzes mit mindestens einer Mineralsäure, um eine Waschlösung zu bilden, welche mindestens ein Seltene-Erdenelement und ein festes Material aufweist;
    Trennen des festen Materials von der Waschlösung;
    Hinzufügen einer Oxalsäure zu der Waschlösung, um ein Seltene-Erdenoxalatkonzentrat auszuscheiden bzw. zu fällen;
    Aufheizen des Seltene-Erdenoxalatkonzentrates in Luft, um ein Oxyd des Seltene-Erdenkonzentrates zu bilden;
    Mischen des Oxydes des Seltene-Erdenkonzentrates mit einem Ammoniumsalz und Aufheizen in Luft, um anhydrische bzw. wasserfreie Seltene-Erdensalze zu bilden;
    Bilden einer Mischung der anhydrischen Seltene-Erdensalze in einer wässrigen Lösung; und
    Trennen der Seltene-Erdenelemente von der wässrigen Lösung durch ein Stromgewinnungsverfahren unter Verwendung einer Opferanode.
  3. Verfahren nach Anspruch 2, wobei die Mineralsäure eine Konzentration mit einem pH-Wert von weniger als 1 hat.
  4. Verfahren nach Anspruch 3, wobei die Mineralsäure aus der Gruppe von Mineralsäuren ausgewählt ist, welche HCl, HNO3 und H2SO4 aufweist.
  5. Verfahren nach Anspruch 2, wobei das Verfahren weiter den Schritt aufweist, zumindest ein Metallion aus der Waschlösung zu entfernen.
  6. Verfahren nach Anspruch 5, wobei der Schritt des Entfernens von mindestens einem Metallion aus der Waschlösung weiter das Titrieren mit Magnesiumoxyd (MgO) auf einen pH-Wert von 14 aufweist.
  7. Verfahren nach Anspruch 2, wobei der Schritt des Hinzufügens von Oxalsäure durch den Schritt des Titrierens mit Magnesiumoxyd ersetzt wird.
  8. Verfahren nach Anspruch 2, wobei der Schritt des Hinzufügens von Oxalsäure durch den Schritt des Titrierens mit Magnesiumoxyd auf einen pH-Wert von 7 ersetzt wird, um Seltene-Erdenhydroxyd zu erzeugen.
  9. Verfahren nach Anspruch 2, wobei der Schritt des Hinzufügens von Oxalsäure durch den Schritt des Titrierens mit einem Karbonat auf einen pH-Wert von 7 ersetzt wird, um Karbonatkonzentrat zu erzeugen.
  10. Verfahren zum Extrahieren von Seltene-Erdenelementen aus einem Erzmaterial, welches Seltene-Erdenelemente enthält, wobei das Verfahren die folgenden Schritte aufweist:
    Auswaschen bzw. Laugen des Erzmaterials mit einer Mineralsäurelösung, wobei die Mineralsäurelösung eine Oxalatverbindung aufweist;
    Rühren der Mineralsäurelösung, um die Seltene-Erdenelemente aus dem Erzmaterial zu lösen;
    Trennen des gelösten Erzmaterials von der Mineralsäurelösung;
    Titrieren mit einer Base, um ein Seltene-Erdenoxalatkonzentrat zu erzeugen;
    Entfernen von mindestens einem Metallion aus dem Seltene-Erdenoxalatkonzentrat;
    Hinzufügen von Oxalsäure, um ein Seltene-Erdenoxalatkonzentrat auszuscheiden bzw. zu fällen;
    Aufheizen des Seltene-Erdenoxalatkonzentrats in Luft, um ein Oxyd des Seltene-Erdenkonzentrates zu bilden;
    Mischen des Oxydes der Seltene-Erdenelemente mit einem Ammoniumsalz und Aufheizen, um anhydrische bzw. wasserfreie Seltene-Erdensalze zu bilden;
    Bilden einer Mischung von anhydrischen Seltene-Erdensalzen in einer wässrigen Lösung; und
    Trennen der Seltene-Erdenelemente von der wässrigen Lösung durch ein Stromgewinnungsverfahren unter Verwendung einer Opferanode.
  11. Verfahren nach Anspruch 10, wobei die Oxalatverbindung Ammoniumoxalat aufweist.
  12. Verfahren nach Anspruch 10, wobei die Base aus Magnesiumoxyd besteht.
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